Cleared Traditional

K874157 - LASE EVACUATOR/ASPIRATOR

K874157 is an FDA 510(k) clearance for LASE EVACUATOR/ASPIRATOR, manufactured by Lase, Inc.. The device is a Class 2 General & Plastic Surgery device with product code BTA cleared through the Traditional 510(k) pathway after a 160-day FDA review.

K874157 · Lase, Inc. · General & Plastic Surgery device
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Mar 1988
Decision
160d
Days
Class 2
Risk

K874157 is an FDA 510(k) clearance for the LASE EVACUATOR/ASPIRATOR. Classified as Pump, Portable, Aspiration (manual Or Powered) (product code BTA), Class II - Special Controls.

Submitted by Lase, Inc. (Washington, US). The FDA issued a Cleared decision on March 21, 1988 after a review of 160 days - an extended review cycle.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4780 - the FDA general and plastic surgery device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the General & Plastic Surgery review framework, consistent with the majority of Class II 510(k) submissions.

View all Lase, Inc. devices

FDA 510(k) Submission Details - K874157

510(k) Number K874157 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received October 13, 1987
Decision Date March 21, 1988
Days to Decision 160 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
45d slower than avg
Panel avg: 115d · This submission: 160d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

BTA Device Classification - Class 2, Special Controls

Product Code BTA Pump, Portable, Aspiration (manual Or Powered)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.4780
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most General & Plastic Surgery devices follow this clearance model.

Regulatory Peers - BTA Pump, Portable, Aspiration (manual Or Powered)

All 108
Devices cleared under the same product code (BTA) and FDA review panel - the closest regulatory comparables to K874157.
INTELIJET SUCTION SUPPLY
K922176 · Smith & Nephew Dyonics, Inc. · Nov 1992
AUTOVAC
K921107 · Life Support Products, Inc. · Sep 1992
VACPAC PORTABLE ASPIRATION SYSTEM
K910271 · Jedmed Instrument Co. · Mar 1991
BUNN MODEL 530 ASPIRATOR
K870094 · The John Bunn Co. · Mar 1987
HEAVY DUTY (HD) SUCTION UNITS (W/CANNULAS)
K862569 · Jedmed Instrument Co. · Aug 1986
PORTASPIR II
K851560 · Roseburg SA · Dec 1985